Variant (rsID / SNP)

rs118101777

rs118101777 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IDH2. Location: chromosome 15, position 90,630,704. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

IDH2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:90630704
Cytoband: 15q26.1
HGVS: NM_002168.4(IDH2):c.782G>A (p.Arg261His)
Allele change: Missense_R261H

Associated conditions / phenotypes

D-2-hydroxyglutaric aciduria 2

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.